Variant #0000982658 (NC_000017.10:g.57076830A>C, NC_000017.10(NM_015294.3):c.2813-10T>G (TRIM37))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.57076830A>C
DNA change (hg38) -
Published as TRIM37(NM_015294.6):c.2813-10T>G
ISCN -
DB-ID TRIM37_000076
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRIM37 NM_001005207.2 -?/. - c.2813-10T>G r.(=) p.(=)
PPM1E NM_014906.4 -?/. - c.*18438A>C r.(=) p.(=)
TRIM37 NM_015294.3 -?/. - c.2813-10T>G r.(=) p.(=)


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